Evidence map›Paper›PMID 19484130›Full record

ArticlePloS one2009

Gene classification based on amino acid motifs and residues: the DLX (distal-less) test case.

Nuno A Fonseca, Cristina P Vieira, Jorge Vieira

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Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Nuno A FonsecaInstituto de Biologia Molecular e Celular (IBMC), University of Porto, Porto, Portugal.
Cristina P Vieira
Jorge Vieira

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComparative studies using hundreds of sequences can give a detailed picture of the evolution of a given gene family. Nevertheless, retrieving only the sequences of interest from public databases can be difficult, in particular, when working with highly divergent sequences. The difficulty increases substantially when one wants to include in the study sequences from many (or less well studied) species whose genomes are non-annotated or incompletely annotated. METHODOLOGY/PRINCIPAL

findingsIn this work we evaluate the usefulness of different approaches of gene retrieval and classification, using the distal-less (DLX) gene family as a test case. Furthermore, we evaluate whether the use of a large number of gene sequences from a wide range of animal species, the use of multiple alternative alignments, and the use of amino acids aligned with high confidence only, is enough to recover the accepted DLX evolutionary history. CONCLUSIONS/SIGNIFICANCE: The canonical DLX homeobox gene sequence here derived, together with the characteristic amino acid variants here identified in the DLX homeodomain region, can be used to retrieve and classify DLX genes in a simple and efficient way. A program is made available that allows the easy retrieval of synteny information that can be used to classify gene sequences. Maximum likelihood trees using hundreds of sequences can be used for gene identification. Nevertheless, for the DLX case, the proposed DLX evolutionary is not recovered even when multiple alignment algorithms are used.

Indexed as

AlgorithmsAmino AcidsAnimalsBiological EvolutionCodonComputational BiologyEvolution, MolecularGenomeHomeodomain ProteinsHumansLikelihood FunctionsModels, GeneticMultigene FamilyPhylogenyTranscription FactorsVertebratesAmino AcidsCodonDistal-less homeobox proteinsHomeodomain ProteinsTranscription Factors

Identifiers

PMID19484130
PMCPMC2685005

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.